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Laboratory Equipment Validation Specialist

182 días · Listado muy antiguo

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Original en inglés
The Laboratory Equipment Validation Specialist is responsible for the validation and lifecycle management of laboratory equipment used in a regulated pharmaceutical environment. This role ensures compliance with cGMP regulations through the planning, execution, and documentation of validation activities for analytical instruments, with a strong focus on UPLC systems and densitometer. The specialist will support laboratory operations by maintaining validated states and ensuring data integrity and regulatory

Características

Compliance With Cgmp Regulations Strong Focus On Uplc Systems And Densitometer Maintaining Validated States Ensuring Data Integrity And Regulatory Compliance
Empresa QRC GROUP LLC
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